FDA.reportPublic FDA data

FungiFree Antifungal Ringworm Cream

Manufacturer
YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD
Effective date
2024-03-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:09:51

Label at a glance#

ProductFungiFree Antifungal Ringworm Cream
Active ingredientMENTHOL, UNSPECIFIED FORM, SILVER, MICONAZOLE
Label structure8 sections

Indications and uses

Targets Athletes Foot, Psoriasis, Eczema, Ringworm, and Fungal Infections. Relieves itching, irritation, redness, scaling and discomfort.

Dosage and administration

Clean and dry the affected area. Apply a thin layer of cream 3-4 times daily. Use daily for 4 weeks. If your condition persists, see a doctor. This product is not effective on the scalp or nails. Avoid applying it to the face.

Label contents#

Full prescribing information#

Active Ingredient                               Purpose

OTC - ACTIVE INGREDIENT SECTION

Menthol 8.0%…............................…………………..………………….Anti-Fungal
Colloidal Silver 0.1%…............................……..…..………………….Anti-Fungal
Miconazole 0.1%…............................…………….……..…………….Anti-Fungal

Uses

INDICATIONS & USAGE SECTION

Targets Athletes Foot, Psoriasis, Eczema, Ringworm, and Fungal Infections. Relieves itching, irritation, redness, scaling and discomfort.

Warnings

WARNINGS SECTION

For external use only

Do not use onchildren under 3 years of age unless directed by a doctor.

When using this productavoid contact with eyes.

Stop and ask a doctor if- irritation occurs - there is no improvement within 4 weeks

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean and dry the affected area.
  • Apply a thin layer of cream 3-4 times daily.
  • Use daily for 4 weeks.
  • If your condition persists, see a doctor.
  • This product is not effective on the scalp or nails. Avoid applying it to the face.

Other information

SPL UNCLASSIFIED SECTION

Store away from excess heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Chlorhexidine Diacetate, Sophora Angustifolia, Dictamnus Dasycarpus, Kochia Scoparia, Lonicera Japonica, Chrysanthemum Indicum, Phellodendron Amurense, Cnidii Fructus, Petroleum Jelly, Glycerol, Stearic Acid, Cetostearyl Alcohol, Azone, Allantoin, Glycerol Monostearate

Questions or comments?

SPL UNCLASSIFIED SECTION

Contact us at support@fungifree.com

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MICONAZOLE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3a55f4fb-5aec-4c88-0ff7-4d608ad4866aProduct name120140508
5b9a7965-36d2-8412-dcaf-f76a65411611Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83364-003-01FungiFree Antifungal Ringworm Cream50 g in 1 JARCREAM501
83364-003-01FungiFree Antifungal Ringworm Cream1 in 1 BOXCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83364-003FUNGIFREE ANTIFUNGAL RINGWORM CREAM (MENTHOL,COLLOIDAL SILVER,MICONAZOLE) CREAM [YITONGBADA (SHENZHEN) INTERNATIONAL TRADE CO., LTD]12 package rows20240316_a8c848e2-1be3-4fc6-8f3b-80aa3db990e6.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83364-00383364-003-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLORHEXIDINE ACETATE5908ZUF22YIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
DICTAMNUS DASYCARPUS ROOT6153LEN214IACT
BASSIA SCOPARIA WHOLE240G38P85ZIACT
LONICERA JAPONICA STEMNW9XC3TM8RIACT
CHRYSANTHEMUM INDICUM FLOWERI6OER6U04LIACT
PHELLODENDRON AMURENSE BARKPBG27B754GIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
PETROLATUM4T6H12BN9UIACT
GLYCERINPDC6A3C0OXIACT
STEARIC ACID4ELV7Z65APIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
LAUROCAPRAM1F3X9DRV9XIACT
ALLANTOIN344S277G0ZIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB
SILVER3M4G523W1GACTIB
MICONAZOLE7NNO0D7S5MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
13b6bd75-7750-f4b1-e063-6294a90a10f4a8c848e2-1be3-4fc6-8f3b-80aa3db990e62024-03-15WarningsExact identifier
spl id: 13b6bd75-7750-f4b1-e063-6294a90a10f4
spl set id: a8c848e2-1be3-4fc6-8f3b-80aa3db990e6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.